Canonical Allele Identifier: CA15559003
Gene: EBF2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11135910

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.26034626C>T , CM000670.2:g.26034626C>T GRCh38
NC_000008.10:g.25892142C>T , CM000670.1:g.25892142C>T GRCh37
NC_000008.9:g.25948059C>T NCBI36
NG_030344.1:g.15499G>A

Transcript Alleles

HGVS Amino-acid change
NM_022659.3:c.483-1473G>A VV NP_073150.2:p.=
ENST00000408929.7:c.39-1473G>A ENSP00000386178.3:p.=
ENST00000517825.1:n.802-1473G>A
ENST00000520164.5:c.483-1473G>A ENSP00000430241.1:p.=